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肌醇1,4,5-三磷酸作用的阈值

Threshold for inositol 1,4,5-trisphosphate action.

作者信息

Missiaen L, De Smedt H, Parys J B, Sienaert I, Valingen S, Casteels R

机构信息

Laboratorium voor Flysiologie, Leuven, Belgium.

出版信息

J Biol Chem. 1996 May 24;271(21):12287-93. doi: 10.1074/jbc.271.21.12287.

Abstract

We developed a unidirectional 45Ca2+ efflux technique in which 60 cumulative doses of inositol 1,4,5-trisphosphate (InsP3), each lasting 6 s, were subsequently added to permeabilized A7r5 cells. This technique allowed an accurate determination of the threshold for InsP3 action, which was around 32 nM InsP3 under control conditions. The InsP3-induced Ca2+ release was characterized by an initial rapid phase, after which the normalized rate progressively decreased. The slowing of the release was associated with a shift of the threshold to higher InsP3 concentrations. Stimulatory concentrations of thimerosal (10 microM) shifted the threshold to 4.5 nM InsP3 and increased both the cooperativity and the maximal normalized rate of Ca2+ release. This low threshold was maintained when the thimerosal concentration was increased to inhibitory levels (100 microM) but then the effects on the cooperativity and on the normalized rate of Ca2+ release disappeared. Oxidized glutathione (5 mM) was much less effective in stimulating the release and did not have an effect on the threshold or on the cooperativity. ATP (5 mM) stimulated the release despite a shift in threshold toward higher InsP3 concentrations. Luminal Ca2+ did not affect the threshold for InsP3 action but stimulated the normalized release at each InsP3 concentration. The inhibitory effect of 10 microM free cytosolic Ca2+ was associated with a shift in threshold to higher InsP3 concentrations and a decreased cooperativity of the release process. We conclude that this novel technique of accurately measuring the threshold for InsP3 action under various experimental conditions has allowed us to refine the analysis of the kinetic parameters involved in the regulation of the InsP3 receptor.

摘要

我们开发了一种单向45Ca2+外流技术,在该技术中,随后向透化的A7r5细胞中添加60次累积剂量的肌醇1,4,5-三磷酸(InsP3),每次持续6秒。该技术能够准确测定InsP3作用的阈值,在对照条件下,该阈值约为32 nM InsP3。InsP3诱导的Ca2+释放的特征是初始快速阶段,之后归一化速率逐渐降低。释放速率的减慢与阈值向更高InsP3浓度的转变有关。刺激浓度的硫柳汞(10 microM)将阈值转变为4.5 nM InsP3,并增加了Ca2+释放的协同性和最大归一化速率。当硫柳汞浓度增加到抑制水平(100 microM)时,这种低阈值得以维持,但随后对协同性和Ca2+释放归一化速率上的影响消失。氧化型谷胱甘肽(5 mM)在刺激释放方面效果要差得多,并且对阈值或协同性没有影响。ATP(5 mM)尽管阈值向更高的InsP3浓度偏移,但仍刺激了释放。管腔Ca2+不影响InsP3作用的阈值,但在每个InsP3浓度下都刺激了归一化释放。10 microM游离胞质Ca2+的抑制作用与阈值向更高InsP3浓度的转变以及释放过程协同性的降低有关。我们得出结论,这种在各种实验条件下准确测量InsP3作用阈值的新技术使我们能够完善对InsP3受体调节中涉及的动力学参数的分析。

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